Pediatric rheumatology

Clinical outcomes of giant coronary aneurysms in South Asian children with Kawasaki disease

Pediatr Rheumatol Online JPublished Retrospective cohort study

Authors' conclusion

Delayed diagnosis and treatment intensification may have contributed to mixed outcomes in this GCAA cohort.

Study context

Population
Children with kawasaki disease (KD)-associated giant coronary artery aneurysms (GCAAs) (z-score >10 or diameter >8mm), referred with documented IVIg resistance, treated 2019–2024 at a tertiary care center in Kerala, Indiatwo lost-to-follow-up
Participants
18 children
Outcome
GCAA dimension change
Follow-up
Last
Methodological detailssingle tertiary care centre
  • Single tertiary care centre

Main finding

As reported in the abstract

median follow-up 8.6 (5.2 - 19.4) months

Complete GCAA resolution

three (18.8%)

Reduction to small/medium aneurysms

six (37.6%)

Remained static

five (31.3%)

Observational data: associations, not effects.

Secondary outcomes

Anticoagulation discontinued (children whose aneurysms resolved or reduced significantly)

Anticoagulation discontinued
56.25%

Delayed diagnosis (>10 days after symptom onset)

Delayed diagnosis
ten (55%)
Median diagnosis, days
11 (IQR 7 - 13.5)
All faced delays in treatment intensification

Mortality

Death from MI
One (6.3%)

Safety

Coronary artery bypass grafting

Patient requiring CABG
1

Original publication

Clinical outcomes of giant coronary aneurysms in South Asian children with Kawasaki disease. Pediatr Rheumatol Online J. Published 29 December 2025. doi:10.1186/s12969-025-01178-0

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